|
ENST00000224721.12:c.8182G>T
MANE Select
|
ENSP00000224721.9:p.Gly2728Cys
|
|
|
ENST00000642965.1:c.2115G>T
|
ENSP00000495222.1:n.2115G>T
|
|
|
ENST00000647092.1:c.1779G>T
|
ENSP00000495176.1:n.1779G>T
|
|
|
ENST00000224721.10:c.8197G>T
|
ENSP00000224721.8:p.Gly2733Cys
|
|
|
ENST00000398788.4:c.1462G>T
|
ENSP00000381768.3:p.Gly488Cys
|
|
|
ENST00000475158.1:n.1718G>T
|
|
|
|
ENST00000619887.4:c.1462G>T
|
ENSP00000478374.1:p.Gly488Cys
|
|
|
ENST00000622827.4:c.8182G>T
|
ENSP00000483211.1:p.Gly2728Cys
|
|
|
NM_001171933.1:c.1462G>T
|
NP_001165404.1:p.Gly488Cys
|
|
|
NM_001171934.1:c.1462G>T
|
NP_001165405.1:p.Gly488Cys
|
|
|
NM_022124.5:c.8182G>T
|
NP_071407.4:p.Gly2728Cys
|
|
|
XM_006717940.2:c.8377G>T
|
XP_006718003.1:p.Gly2793Cys
|
|
|
XM_006717942.2:c.8311G>T
|
XP_006718005.1:p.Gly2771Cys
|
|
|
XM_011540039.1:c.8374G>T
|
XP_011538341.1:p.Gly2792Cys
|
|
|
XM_011540040.1:c.8371G>T
|
XP_011538342.1:p.Gly2791Cys
|
|
|
XM_011540041.1:c.8317G>T
|
XP_011538343.1:p.Gly2773Cys
|
|
|
XM_011540042.1:c.8287G>T
|
XP_011538344.1:p.Gly2763Cys
|
|
|
XM_011540043.1:c.8377G>T
|
XP_011538345.1:p.Gly2793Cys
|
|
|
XM_011540044.1:c.8242G>T
|
XP_011538346.1:p.Gly2748Cys
|
|
|
XM_011540045.1:c.8377G>T
|
XP_011538347.1:p.Gly2793Cys
|
|
|
XM_011540046.1:c.7837G>T
|
XP_011538348.1:p.Gly2613Cys
|
|
|
XM_011540047.1:c.7195G>T
|
XP_011538349.1:p.Gly2399Cys
|
|
|
XM_011540052.1:c.4705G>T
|
XP_011538354.1:p.Gly1569Cys
|
|
|
NM_022124.6:c.8182G>T
MANE Select
|
NP_071407.4:p.Gly2728Cys
|
|
